# nilotinib

NDC: 72205-239
Generic name: nilotinib
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20251119

FDA application: ANDA218544

## Active ingredients

- NILOTINIB: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72205-239"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-239
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=13b46e09-62d2-4ce9-b3c0-deafcb1f1842